Pramoxine Hydrochloride Anorectal
- Dosage form
- LOTION
- Labeler
- Stratus Pharmaceuticals
- Label updated
- 2025-10-02
- Retrieved
- 2026-09-07
- Active ingredients
- Pramoxine Hydrochloride
Label information
Drug Facts
Active ingredient
Pramoxine HCL 1% w/w
Purpose
Local Anesthetic
Use
- for the temporary relief of itching and discomfort in the perianal area.
Warnings
for external use only.
Do not
- exceed the recommended daily dosage unless directed by a Physician.
Do not
- put this product into rectum by using fingers or any applicator.
Stop use and ask a Physician if
- Condition worsens
- Symptoms do not improve in 7 days
- Allergic reactions develop to ingredients in this product
- Symptoms being treated do not improve or subsideor if redness, irritation, swelling, pain, bleeding or other symptoms develop or increase
Label information
Keep this product out of the reach of children. If swallowed, get medical attention or contact a Poison Control Center right away.
Directions
- Shake well before using.
- When practical, cleansethe affected area with mild soap and warm water and rinse thoroughly.
- Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
- Adults and children 12 years of age and older: apply to affected area up to five times daily.
- Children under 12 years of age, consult a Physician.
Inactive ingredients
Carbomer 940, Cetyl Alcohol, Di-isopropyl Adipate, Dimethicone, Glycerin 99.7%, Lanolin Anhydrous, Light Mineral Oil, PEG 40 Stearate, Potassium Sorbate, Purified Water, Sorbic Acid, Stearic Acid, Stearyl Alcohol, Trolamine, Ultimate White Petrolatum.
Questions or comments?
Call us at: 1-800-442-7882
Label information
Distributed by:
STRATUS
PHARMACEUTICALS INC
Miami, Florida 33186
PRINCIPAL DISPLAY PANEL - 118 mL Bottle Box
NDC 58980-522-40
ANORECTAL
PRAMOXINE
HYDROCHLORIDE 1%
ANORECTAL
FAST RELIEF FROM ITCH
AND DISCOMFORT
ANORECTAL
(hemorrhoidal)
LOTION
Net 4 fl oz (118 mL)
[Image in the official label — see DailyMed source]
DailyMed Set ID: 39a16b66-b0e9-412f-8773-8dec0a1227e0 · Version 1
NDC: 58980-522